scholarly journals Decadal regional air quality simulations over Europe in present climate: near surface ozone sensitivity to external meteorological forcing

2010 ◽  
Vol 10 (23) ◽  
pp. 11805-11821 ◽  
Author(s):  
E. Katragkou ◽  
P. Zanis ◽  
I. Tegoulias ◽  
D. Melas ◽  
I. Kioutsioukis ◽  
...  
Keyword(s):  
Air Quality ◽  
Solar Radiation ◽  
Boundary Conditions ◽  
Surface Ozone ◽  
Regional Climate ◽  
Radiation Temperature ◽  
Meteorological Forcing ◽  
Near Surface ◽  
The Impact ◽  
Selection Of

Abstract. Regional climate-air quality decadal simulations over Europe were carried out with the RegCM3/CAMx modeling system for the time slice 1991–2000, in order to study the impact of different meteorological forcing on surface ozone. The RegCM3 regional climate model was firstly constrained by the ERA40 reanalysis dataset which is considered as an experiment with perfect meteorological boundary conditions and then it was constrained by the global circulation model ECHAM5. A number of meteorological parameters were examined including the 500 mb geopotential height, solar radiation, temperature, cloud liquid water path, planetary boundary layer height and surface wind. The different RegCM meteorological forcing resulted in changes of near surface ozone over Europe ranging between ± 4 ppb for winter and summer. The area showing the greatest sensitivity in O3 during winter is central and southern Europe while in summer central north continental Europe. The different meteorological forcing impacts on the atmospheric circulation, which in turn affects cloudiness and solar radiation, temperature, wind patterns and the meteorology depended biogenic emissions. For comparison reasons, the impact of chemical boundary conditions on surface ozone was additionally examined with a series of sensitivity studies, indicating that surface ozone changes are comparable to those caused by the different meteorological forcing. These findings suggest that, when it comes to regional climate-air quality simulations, the selection of external meteorological forcing can be as important as the selection of adequate chemical lateral boundary conditions.

Evaluating the impact of chemical boundary conditions on near surface ozone in regional climate–air quality simulations over Europe

2013 ◽  
Vol 134 ◽  
pp. 116-130 ◽  
Author(s):  
D. Akritidis ◽  
P. Zanis ◽  
E. Katragkou ◽  
M.G. Schultz ◽  
I. Tegoulias ◽  
...  
Keyword(s):  
Air Quality ◽  
Boundary Conditions ◽  
Surface Ozone ◽  
Regional Climate ◽  
Near Surface ◽  
The Impact

scholarly journals The regional impact of urban emissions on air quality in Europe: the role of the urban canopy effects

2021 ◽  
Vol 21 (18) ◽  
pp. 14309-14332
Author(s):  
Peter Huszar ◽  
Jan Karlický ◽  
Jana Marková ◽  
Tereza Nováková ◽  
Marina Liaskoni ◽  
...  
Keyword(s):  
Air Quality ◽  
Land Surface ◽  
Climate Models ◽  
Regional Climate ◽  
Regional Scale ◽  
Urban Canopy ◽  
Regional Climate Models ◽  
Near Surface ◽  
Urban Emissions ◽  
The Impact

Abstract. Urban areas are hot spots of intense emissions, and they influence air quality not only locally but on a regional or even global scale. The impact of urban emissions over different scales depends on the dilution and chemical transformation of the urban plumes which are governed by the local- and regional-scale meteorological conditions. These are influenced by the presence of urbanized land surface via the so-called urban canopy meteorological forcing (UCMF). In this study, we investigate for selected central European cities (Berlin, Budapest, Munich, Prague, Vienna and Warsaw) how the urban emission impact (UEI) is modulated by the UCMF for present-day climate conditions (2015–2016) using two regional climate models, the regional climate models RegCM and Weather Research and Forecasting model coupled with Chemistry (WRF-Chem; its meteorological part), and two chemistry transport models, Comprehensive Air Quality Model with Extensions (CAMx) coupled to either RegCM and WRF and the “chemical” component of WRF-Chem. The UCMF was calculated by replacing the urbanized surface by a rural one, while the UEI was estimated by removing all anthropogenic emissions from the selected cities. We analyzed the urban-emission-induced changes in near-surface concentrations of NO2, O3 and PM2.5. We found increases in NO2 and PM2.5 concentrations over cities by 4–6 ppbv and 4–6 µg m−3, respectively, meaning that about 40 %–60 % and 20 %–40 % of urban concentrations of NO2 and PM2.5 are caused by local emissions, and the rest is the result of emissions from the surrounding rural areas. We showed that if UCMF is included, the UEI of these pollutants is about 40 %–60 % smaller, or in other words, the urban emission impact is overestimated if urban canopy effects are not taken into account. In case of ozone, models due to UEI usually predict decreases of around −2 to −4 ppbv (about 10 %–20 %), which is again smaller if UCMF is considered (by about 60 %). We further showed that the impact on extreme (95th percentile) air pollution is much stronger, and the modulation of UEI is also larger for such situations. Finally, we evaluated the contribution of the urbanization-induced modifications of vertical eddy diffusion to the modulation of UEI and found that it alone is able to explain the modeled decrease in the urban emission impact if the effects of UCMF are considered. In summary, our results showed that the meteorological changes resulting from urbanization have to be included in regional model studies if they intend to quantify the regional footprint of urban emissions. Ignoring these meteorological changes can lead to the strong overestimation of UEI.

scholarly journals The regional impact of urban emissions on air quality in Europe: the role of the urban canopy effects

2021 ◽  
Author(s):  
Peter Huszar ◽  
Jan Karlický ◽  
Jana Marková ◽  
Tereza Nováková ◽  
Marina Liaskoni ◽  
...  
Keyword(s):  
Air Quality ◽  
Rural Areas ◽  
Land Surface ◽  
Urban Areas ◽  
Regional Climate ◽  
Regional Scale ◽  
Urban Canopy ◽  
Near Surface ◽  
Urban Emissions ◽  
The Impact

Abstract. Urban areas are hot-spots of intense emissions and they influence air-quality not only locally but on regional or even global scales. The impact of urban emissions over different scales depends on the dilution and chemical transformation of the urban plumes which are governed by the local and regional scale meteorological conditions. These are influenced by the presence of urbanized land-surface via the so called urban canopy meteorological forcing (UCMF). In this study, we investigate for selected central European cities (Berlin, Budapest, Munich, Prague, Vienna and Warsaw), how the urban emission impact (UEI) is modulated by the UCMF for present day climate conditions (2015–2016) using three regional climate-chemistry models: the regional climate models RegCM and WRF-Chem (its meteorological part), the chemistry transport model CAMx coupled to either RegCM and WRF and the “chemical” component of WRF-Chem. The UCMF was calculated by replacing the urbanized surface by rural one while the UEI was estimated by removing all anthropogenic emissions from the selected cities. We analyzed the urban emissions induced changes of near surface concentrations of NO2, O3 and PM2.5. We found increases of NO2 and PM2.5 concentrations over cities by 4–6 ppbv, and 4–6 μgm−3, respectively meaning that about 40–60 % and 20–40 % of urban concentrations of NO2 and PM2.5 are caused by local emissions and the rest is the result of emissions from surrounding rural areas. We showed that if UCMF is included, the UEI of these pollutants is about 40–60 % smaller, or in other words, the urban emission impact is overestimated if urban canopy effects are not taken into account. In case of ozone, models due to UEI usually predict decreases around −2 to −4 ppbv (about 10–20 %), which is again smaller if UCMF is considered (by about 60 %). We further showed that the impact on extreme (95th percentile) air-pollution is much stronger, as well as the modulation of UEI is larger for such situations. Finally, we evaluated the contribution of the urbanization induced modifications of vertical eddy-diffusion to the modulation of UEI, and found that it alone is able to explain the modelled decrease of the urban emission impact if the effects of UCMF are considered. In summary, our results showed that the meteorological changes resulting from urbanization have to be included in regional model studies if they intend to quantify the regional fingerprint of urban emissions. Ignoring these meteorological changes can lead to strong overestimation of UEI.

Evaluation of near surface ozone in air quality simulations forced by a regional climate model over Europe for the period 1991–2000

2011 ◽  
Vol 45 (36) ◽  
pp. 6489-6500 ◽  
Author(s):  
P. Zanis ◽  
E. Katragkou ◽  
I. Tegoulias ◽  
A. Poupkou ◽  
D. Melas ◽  
...  
Keyword(s):  
Air Quality ◽  
Regional Climate Model ◽  
Climate Model ◽  
Surface Ozone ◽  
Regional Climate ◽  
Near Surface

scholarly journals Decadal regional air quality simulations over Europe in present climate: near surface ozone sensitivity to external meteorological forcing

2009 ◽  
Vol 9 (3) ◽  
pp. 10675-10710 ◽  
Author(s):  
E. Katragkou ◽  
P. Zanis ◽  
I. Tegoulias ◽  
D. Melas ◽  
B. C. Krüger ◽  
...  
Keyword(s):  
Air Quality ◽  
Climate Model ◽  
Surface Ozone ◽  
Winter Season ◽  
Biogenic Emissions ◽  
Meteorological Forcing ◽  
Near Surface ◽  
Ozone Sensitivity ◽  
Regional Air Quality ◽  
Induced Changes

Abstract. Regional air quality decadal simulations were carried out using the air quality model CAMx driven off-line by the regional climate model RegCM3 for the time slice 1991–2000 using two different datasets of external meteorological forcing to constrain RegCM3: the ERA40 global atmospheric reanalysis dataset and the output from the GCM ECHAM5. The focus of this work is to compare the perfect lateral boundary conditions experiment with the GCM driven control experiment and to investigate how this external meteorological forcing affects near surface ozone. The different RegCM3 meteorological forcings resulted in changes of near surface ozone over Europe ranging between ±5 ppb for winter and summer, while all model parameterizations and anthropogenic emissions remained unchanged. Changes in near surface ozone are induced by changes in meteorological fields and biogenic emissions, which are on-line calculated and meteorology-dependent. The model simulations suggest that the change in solar radiation is the factor that mostly modulates the ozone changes in summer. During winter season it is found that the induced changes in NOx explain about 40% of the ozone variability. The meteorological induced changes in biogenic emissions are quite low for winter with rather small impact on ozone while they are more temperature than radiation dependent. Using multiple regression analysis to associate the changes in near surface ozone with the respective changes in selected meteorological parameters and ozone precursors, an explained variance of 70% in summer and 60% in winter is reproduced.

scholarly journals Assessing the regional impacts of Mexico City emissions on air quality and chemistry

2009 ◽  
Vol 9 (11) ◽  
pp. 3731-3743 ◽  
Author(s):  
M. Mena-Carrasco ◽  
G. R. Carmichael ◽  
J. E. Campbell ◽  
D. Zimmerman ◽  
Y. Tang ◽  
...  
Keyword(s):  
Air Quality ◽  
Mexico City ◽  
Ozone Production ◽  
Anthropogenic Aerosol ◽  
Near Surface ◽  
Mixing Ratios ◽  
Regional Impacts ◽  
Photolysis Rates ◽  
Regional Air Quality ◽  
The Impact

Abstract. The impact of Mexico City (MCMA) emissions is examined by studying its effects on air quality, photochemistry, and on ozone production regimes by combining model products and aircraft observations from the MILAGRO experiment during March 2006. The modeled influence of MCMA emissions to enhancements in surface level NOx, CO, and O3 concentrations (10–30% increase) are confined to distances <200 km, near surface. However, the extent of the influence is significantly larger at higher altitudes. Broader MCMA impacts (some 900 km Northeast of the city) are shown for specific outflow conditions in which enhanced ozone, NOy, and MTBE mixing ratios over the Gulf of Mexico are linked to MCMA by source tagged tracers and sensitivity runs. This study shows that the "footprint" of MCMA on average is fairly local, with exception to reactive nitrogen, which can be transported long range in the form of PAN, acting as a reservoir and source of NOx with important regional ozone formation implications. The simulated effect of MCMA emissions of anthropogenic aerosol on photochemistry showed a maximum regional decrease of 40% in J[NO2→NO+O], and resulting in the reduction of ozone production by 5–10%. Observed ozone production efficiencies are evaluated as a function of distance from MCMA, and by modeled influence from MCMA. These tend to be much lower closer to MCMA, or in those points where modeled contribution from MCMA is large. This research shows that MCMA emissions do effect on regional air quality and photochemistry, both contributing large amounts of ozone and its precursors, but with caveat that aerosol concentrations hinder formation of ozone to its potential due to its reduction in photolysis rates.

scholarly journals Modelling the impact of megacities on local, regional and global tropospheric ozone and the deposition of nitrogen species

2013 ◽  
Vol 13 (24) ◽  
pp. 12215-12231 ◽  
Author(s):  
Z. S. Stock ◽  
M. R. Russo ◽  
T. M. Butler ◽  
A. T. Archibald ◽  
M. G. Lawrence ◽  
...  
Keyword(s):  
Air Quality ◽  
Urban Areas ◽  
Climate Model ◽  
Surface Ozone ◽  
Global Scale ◽  
Chemical Environment ◽  
Ozone Production ◽  
The Uk ◽  
The Impact ◽  
Local Emissions

Abstract. We examine the effects of ozone precursor emissions from megacities on present-day air quality using the global chemistry–climate model UM-UKCA (UK Met Office Unified Model coupled to the UK Chemistry and Aerosols model). The sensitivity of megacity and regional ozone to local emissions, both from within the megacity and from surrounding regions, is important for determining air quality across many scales, which in turn is key for reducing human exposure to high levels of pollutants. We use two methods, perturbation and tagging, to quantify the impact of megacity emissions on global ozone. We also completely redistribute the anthropogenic emissions from megacities, to compare changes in local air quality going from centralised, densely populated megacities to decentralised, lower density urban areas. Focus is placed not only on how changes to megacity emissions affect regional and global NOx and O3, but also on changes to NOy deposition and to local chemical environments which are perturbed by the emission changes. The perturbation and tagging methods show broadly similar megacity impacts on total ozone, with the perturbation method underestimating the contribution partially because it perturbs the background chemical environment. The total redistribution of megacity emissions locally shifts the chemical environment towards more NOx-limited conditions in the megacities, which is more conducive to ozone production, and monthly mean surface ozone is found to increase up to 30% in megacities, depending on latitude and season. However, the displacement of emissions has little effect on the global annual ozone burden (0.12% change). Globally, megacity emissions are shown to contribute ~3% of total NOy deposition. The changes in O3, NOx and NOy deposition described here are useful for quantifying megacity impacts and for understanding the sensitivity of megacity regions to local emissions. The small global effects of the 100% redistribution carried out in this study suggest that the distribution of emissions on the local scale is unlikely to have large implications for chemistry–climate processes on the global scale.

scholarly journals Sensitivity of biogenic volatile organic compounds to land surface parameterizations and vegetation distributions in California

2016 ◽  
Vol 9 (5) ◽  
pp. 1959-1976 ◽  
Author(s):  
Chun Zhao ◽  
Maoyi Huang ◽  
Jerome D. Fast ◽  
Larry K. Berg ◽  
Yun Qian ◽  
...  
Keyword(s):  
Air Quality ◽  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Land Surface ◽  
Aerosol Formation ◽  
Biogenic Volatile Organic Compounds ◽  
Vegetation Map ◽  
Near Surface ◽  
Volatile Organic ◽  
The Impact

Abstract. Current climate models still have large uncertainties in estimating biogenic trace gases, which can significantly affect atmospheric chemistry and secondary aerosol formation that ultimately influences air quality and aerosol radiative forcing. These uncertainties result from many factors, including uncertainties in land surface processes and specification of vegetation types, both of which can affect the simulated near-surface fluxes of biogenic volatile organic compounds (BVOCs). In this study, the latest version of Model of Emissions of Gases and Aerosols from Nature (MEGAN v2.1) is coupled within the land surface scheme CLM4 (Community Land Model version 4.0) in the Weather Research and Forecasting model with chemistry (WRF-Chem). In this implementation, MEGAN v2.1 shares a consistent vegetation map with CLM4 for estimating BVOC emissions. This is unlike MEGAN v2.0 in the public version of WRF-Chem that uses a stand-alone vegetation map that differs from what is used by land surface schemes. This improved modeling framework is used to investigate the impact of two land surface schemes, CLM4 and Noah, on BVOCs and examine the sensitivity of BVOCs to vegetation distributions in California. The measurements collected during the Carbonaceous Aerosol and Radiative Effects Study (CARES) and the California Nexus of Air Quality and Climate Experiment (CalNex) conducted in June of 2010 provided an opportunity to evaluate the simulated BVOCs. Sensitivity experiments show that land surface schemes do influence the simulated BVOCs, but the impact is much smaller than that of vegetation distributions. This study indicates that more effort is needed to obtain the most appropriate and accurate land cover data sets for climate and air quality models in terms of simulating BVOCs, oxidant chemistry and, consequently, secondary organic aerosol formation.

scholarly journals Entrainment and Mixing of Transported Ozone Layers: Implications for Surface Air Quality in the Western U.S.

2020 ◽  
Vol 237 ◽  
pp. 03012
Author(s):  
Christoph Senff ◽  
Andrew Langford ◽  
Raul Alvarez ◽  
Tim Bonin ◽  
Alan Brewer ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Air Quality ◽  
Mixed Layer ◽  
Las Vegas ◽  
Surface Ozone ◽  
Ground Level ◽  
San Joaquin Valley ◽  
Fire Emissions ◽  
Ozone Transport ◽  
The Impact

Recently, two air quality campaigns were conducted in the southwestern United States to study the impact of transported ozone, stratospheric intrusions, and fire emissions on ground-level ozone concentrations. The California Baseline Ozone Transport Study (CABOTS) took place in May – August 2016 covering the central California coast and San Joaquin Valley, and the Fires, Asian, and Stratospheric Transport Las Vegas Ozone Study (FAST-LVOS) was conducted in the greater Las Vegas, Nevada area in May – June 2017. During these studies, nearly 1000 hours of ozone and aerosol profile data were collected with the NOAA TOPAZ lidar. A Doppler wind lidar and a radar wind profiler provided continuous observations of atmospheric turbulence, horizontal winds, and mixed layer height. These measurements allowed us to directly observe the degree to which ozone transport layers aloft were entrained into the boundary layer and to quantify the resulting impact on surface ozone levels. Mixed layer heights in the San Joaquin Valley during CABOTS were generally below 1 km above ground level (AGL), while boundary layer heights in Las Vegas during FAST-LVOS routinely exceeded 3 km AGL and occasionally reached up to 4.5 km AGL. Consequently, boundary layer entrainment was more often observed during FAST-LVOS, while most elevated ozone layers passed untapped over the San Joaquin Valley during CABOTS.

scholarly journals Impacts of future land use and land cover change on mid-21<sup>st</sup>-century surface ozone air quality: Distinguishing between the biogeophysical and biogeochemical effects

2019 ◽  
Author(s):  
Lang Wang ◽  
Amos P. K. Tai ◽  
Chi-Yung Tam ◽  
Mehliyar Sadiq ◽  
Peng Wang ◽  
...  
Keyword(s):  
Land Use ◽  
Air Quality ◽  
Land Cover ◽  
Dry Deposition ◽  
Surface Ozone ◽  
Boreal Summer ◽  
Ozone Pollution ◽  
Lulc Change ◽  
Lulc Changes ◽  
The Impact

Abstract. Surface ozone (O3) is an important air pollutant and greenhouse gas. Land use and land cover (LULC) is one of the critical factors influencing ozone, in addition to anthropogenic emissions and climate. LULC change can on the one hand affect ozone biogeochemically, i.e., via dry deposition and biogenic emissions of volatile organic compounds (VOCs). LULC change can on the other hand alter regional- to large-scale climate through modifying albedo and evapotranspiration, which can lead to changes in surface temperature, hydrometeorology and atmospheric circulation that can ultimately impact ozone biogeophysically over local and remote areas. Such biogeophysical effects of LULC on ozone are largely understudied. This study investigates the individual and combined biogeophysical and biogeochemical effects of LULC on ozone, and explicitly examines the critical pathway for how LULC change impacts ozone pollution. A global coupled atmosphere–chemistry–land model is driven by projected LULC changes from the present day (2000) to future (2050) under RCP4.5 and RCP8.5 scenarios, focusing on the boreal summer. Results reveal that when considering biogeochemical effects only, surface ozone is predicted to have slight changes by up to 2 ppbv maximum in some areas due to LULC changes. It is primarily driven by changes in isoprene emission and dry deposition counteracting each other in shaping ozone. In contrast, when considering the integrated effect of LULC, ozone is more substantially altered by up to 6 ppbv over several regions, reflecting the importance of biogeophysical effects on ozone changes. Furthermore, large areas of these ozone changes are found over the regions without LULC changes where the biogeophysical effect is the only pathway for such changes. The mechanism is likely that LULC change induces a regional circulation response, in particular the formation of anomalous stationary high-pressure systems, shifting of moisture transport, and near-surface warming over the middle-to-high northern latitudes in boreal summer, owing to associated changes in albedo and surface energy budget. Such temperature changes then alter ozone substantially. We conclude that the biogeophysical effect of LULC is an important pathway for the influence of LULC change on ozone air quality over both local and remote regions, even in locations without significant LULC changes. Overlooking the impact of biogeophysical effect may cause evident underestimation of the impacts of LULC change on ozone pollution.

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